FDA inspection
Qingdao London Durex Co., Ltd.: FDA inspection ending Jul 10, 2014
FDA inspection 891775 · No Action Indicated (NAI) · Qingdao
Key facts
| Inspection ID | 891775 |
|---|---|
| Firm | Qingdao London Durex Co., Ltd. |
| FEI number | 3008559248 |
| Address | No. 1-13 Shangma Part, Aodong Road, Chengyang |
| City | Qingdao |
| Country | China |
| Fiscal year | 2014 |
| Inspection end date | Jul 10, 2014 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data